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Bile salts b8631

Manufactured by Merck Group
Sourced in Spain

Bile salts (B8631) are a type of laboratory reagent commonly used in biochemical and biological research. They are a mixture of sodium salts of various bile acids, which are natural surfactants produced by the liver and play a role in the digestion and absorption of fats. As a laboratory product, bile salts are used for a variety of purposes, such as cell lysis, protein solubilization, and the preparation of biological samples for analysis.

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4 protocols using bile salts b8631

1

Aflatoxin B1 Exposure Assessment

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AFB1 standard solution (purity > 99%) was acquired from Sigma-Aldrich (St. Louis, MO, USA). Potassium thiocyanate (KSCN), potassium chloride (KCl), hydrochloric acid (HCl), sodium dihydrogen phosphate (NaH2PO4), sodium hydroxide (NaOH), sodium sulfate (Na2SO4), sodium chloride (NaCl), sodium hydrogen carbonate (Na-HCO3), urea (CO(NH2)2), pepsin A (674 U mg−1 P7000), pancreatin (762 U mg−1 P1750), bile salts (B8631), and α-amylase (930 U mg−1 A3403) were purchased from Sigma-Aldrich (Madrid, Spain). Acetonitrile (ACN) and methanol (MeOH) were obtained from Fisher Scientific (Madrid, Spain). Deionized water was obtained from a Milli-Q water purification system (Millipore, Bedford, MA, USA). Dimethyl sulfoxide (DMSO) was acquired from Fisher Scientific (Geel, Belgium). Bread ingredients were purchased at a local supermarket. Fresh garlic was preserved at 4 °C and minced before use. Propidium iodide (PI) and a cycleTEST™ PLUS DNA Reagent Kit were obtained from BD Biosciences (San Diego, CA, USA) for the cell cycle assay by flow cytometry. The Annexin V–FITC conjugate was acquired from Miltenyi and the MitoTracker® probe was purchased from Invitrogen (Waltham, MA, USA). 2′,7′-dichlorodihydrofluorescein diacetate (H2-DCFDA) and phosphate buffer saline (PBS) were bought from Sigma Chemical Co. (St. Louis, MO, USA).
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2

Aflatoxin B1 and Ochratoxin A Evaluation

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AFB1 and OTA standard solutions (purity > 99%) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Potassium chloride (KCl), potassium thiocyanate (KSCN), sodium dihydrogen phosphate (NaH2PO4), sodium sulfate (Na2SO4), sodium chloride (NaCl), sodium hydrogen carbonate (NaHCO3), urea (CO(NH2)2), α-amylase (930 U mg−1 A3403), hydrochloric acid (HCl), sodium hydroxide (NaOH), formic acid (HCOOH), pepsin A (674 U mg−1 P7000), pancreatin (762 U mg−1 P1750), bile salts (B8631), and phosphate buffer saline (PBS, pH 7.5) were purchased from Sigma-Aldrich (Madrid, Spain). Methanol and ethyl acetate were supplied by Fisher Scientific (Madrid, Spain). Deionized water was purchased from a Milli-Q water purification system (Millipore, Bedford, MA, USA). LAB used in this study (L. plantarum CECT 220) was obtained from the Spanish Type Culture Collection, CECT, Science Park of the University of Valencia (Paterna, València, Spain). The cultures were kept at −80 °C in glycerol 25% until their use.
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3

Analytical Characterization of Hymenocardia Compounds

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Acetonitrile and methanol (HPLC-quality) and ammonia (25%) were supplied by Fisher Chemical. Pepsin (P-7000, from porcine stomach mucosa, 800-2500 U/mg protein), bile salts (B-8631, porcine), pancreatin (76 190, from porcine pancreas, 149 USP U/mg amylase), sodium dihydrogen phosphate anhydrous (NaH2PO4), disodium phosphate dihydrate (Na2HPO4 • 2 H2O) and tris(hydroxymethyl)aminomethane (TRIS) were purchased from Sigma-Aldrich.
Hydrochloric acid (HCl, 32%), sodium bicarbonate (NaHCO3) and sodium hydroxide (NaOH) were obtained from Merck. Formic acid was purchased from Acros Organics. Human liver S9 fraction and NADPH RS (Regenerating System) were purchased from XenoTech. All chemicals and reagents were of analytical grade and in all experiments deionized water (milliQ, Merck Millipore) was used. Hymenocardine (94%) and hymenocardinol (82%) were isolated from root bark of Hymenocardia acida. The purity of these two compounds was determined by HPLC analysis.The analysis was performed using a XBridge C18 column (4.6  250 mm, 5μm, Waters) and water + 0.1% Formic acid (A) and acetonitrile (B) as mobile phase. The flow rate was 1.0 mL/min and the following gradient was applied: 0 to 5 min 80% A and 20% B, 40 to 45 min 100% B. UV detection was done at 201 nm.
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4

Analytical Protocol for Aflatoxin Detection

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Potassium chloride (KCl), potassium thiocyanate (KSCN), sodium dihydrogen phosphate (NaH 2 PO 4 ), sodium sulfate (Na 2 SO 4 ), sodium chloride (NaCl), sodium hydrogen carbonate (NaHCO 3 ), urea (CO(NH 2 ) 2 ), a-amylase (930 U mg À1 A3403), hydrochloric acid (HCl), sodium hydroxide (NaOH), formic acid (HCOOH), pepsin A (674 U mg À1 P7000), pancreatin (762 U mg À1 P1750), bile salts (B8631), phosphate buffer saline (PBS, pH 7.5) and standard solutions of AFB 1 and AFB 2 (!98% purity), were purchased from Sigma-Aldrich (Madrid, Spain). Methanol and ethyl acetate were supplied by Fisher Scientific (Madrid, Spain). Deionized water was purchased from a Milli-Q water purification system (Millipore, Bedford, MA, USA). Chromatographic solvents and water were degassed for 20 min using a Branson 5200 (Branson Ultrasonic Corp., CT, USA) ultrasonic bath.
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